Crouzon Syndrome Latest Advances

Find the Latest Research About Crouzon Syndrome

Last Updated: 06/30/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 7308 publications

Corrigendum to "Hallermann Streiff syndrome: Cranio-facial manifestations systematic review and report of two cases" [J Stomatol Oral Maxillofac Surg 2022;123(4):e219-23].

Corrigendum to "Hallermann Streiff syndrome: Cranio-facial manifestations systematic review and report of two cases" [J Stomatol Oral Maxillofac Surg 2022;123(4):e219-23].

Journal: Journal of stomatology, oral and maxillofacial surgery
Published: June 04, 2026

Progressive Overgrowth of Costochondral Graft in a Case of Hemifacial Microsomia: A Rare and Severe Case.

Progressive Overgrowth of Costochondral Graft in a Case of Hemifacial Microsomia: A Rare and Severe Case.

Journal: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association
Published: June 04, 2026

Impact of Muscular Asymmetry on Velopharyngeal Function in Children with Craniofacial Microsomia: A Pilot Study.

Impact of Muscular Asymmetry on Velopharyngeal Function in Children with Craniofacial Microsomia: A Pilot Study.

Journal: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association
Published: May 28, 2026

Association Between Middle Ear Anomalies and the Severity of Mandibular Deformity in Hemifacial Microsomia.

Association Between Middle Ear Anomalies and the Severity of Mandibular Deformity in Hemifacial Microsomia.

Journal: Ear, nose, & throat journal
Published: May 12, 2026

A case of goldenhar syndrome presenting with entropion

A case of goldenhar syndrome presenting with entropion

Journal: [Zhonghua yan ke za zhi] Chinese journal of ophthalmology
Published: May 08, 2026

Craniometaphyseal dysplasia with severe maxillary hypoplasia due to ANKH gene mutation: A case report.

Craniometaphyseal dysplasia with severe maxillary hypoplasia due to ANKH gene mutation: A case report.

Journal: Journal of genetics
Published: May 05, 2026

The Clinical and Molecular Spectrum of Turkish Patients with Syndromic Craniosynostosis: A Single Center Study.

The Clinical and Molecular Spectrum of Turkish Patients with Syndromic Craniosynostosis: A Single Center Study.

Journal: Turkish archives of pediatrics
Published: May 05, 2026

Left-Sided Mandibular Condylar-Ramus Deficiency Within the Craniofacial Microsomia Spectrum in a 10-Year-Old Patient: A Case Report.

Left-Sided Mandibular Condylar-Ramus Deficiency Within the Craniofacial Microsomia Spectrum in a 10-Year-Old Patient: A Case Report.

Journal: Cureus
Published: April 29, 2026

Case Report: Novel FOXC1 variant c.311T>G (p.Ile104Ser) in a Chinese family with Axenfeld-Rieger syndrome.

Case Report: Novel FOXC1 variant c.311T>G (p.Ile104Ser) in a Chinese family with Axenfeld-Rieger syndrome.

Journal: Frontiers in medicine
Published: April 29, 2026

Ossification of the mandible: A regional composite model of intramembranous, parachondral, and endochondral mechanisms.

Ossification of the mandible: A regional composite model of intramembranous, parachondral, and endochondral mechanisms.

Journal: Archives of oral biology
Published: April 13, 2026

Single-Stage Extracranial Transnasal Repair of Frontoethmoidal Encephalomeningocele Without Coronal Incision.

Single-Stage Extracranial Transnasal Repair of Frontoethmoidal Encephalomeningocele Without Coronal Incision.

Journal: The Journal of craniofacial surgery
Published: April 11, 2026

Hearing rehabilitation in patients with Treacher Collins syndrome.

Hearing rehabilitation in patients with Treacher Collins syndrome.

Journal: Acta oto-laryngologica
Published: April 08, 2026
Showing 1-12 of 7,308

Last Updated: 06/30/2026